Johnson & Johnson Orthopedic Device Recalled Due To Fracture Potential - Huffington P

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Johnson & Johnson Orthopedic Device Recalled Due To Fracture Potential
Huffington Post
Feb 22 (Reuters) - The U.S. Food and Drug Administration on Friday said it has notified healthcare professionals of a Class I recall, the most serious type, of an orthopedic device made by Johnson & Johnson. The device, called LPS Diaphyseal Sleeve, ...
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